Secreted Campylobacter flaggella coregulated proteins as immunogens

ABSTRACT

The invention relates to an immunogenic composition composed of secreted polypeptides derived from  Campylobacter jejuni  non-flagellar proteins that are coordinately expressed with the flagellar regulon. The invention also relates to a method of inducing an immune response to the non-flagellar protein polypeptides.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional application 60/800,099 filed May 12, 2006 and is a divisional application of U.S. patent application Ser. No. 11/800,955 filed May 8, 2007 (U.S. Pat. No. 8,221,764, issued on Jul. 17, 2012).

SEQUENCE LISTING

A written Sequence Listing is included in the Specification showing polypeptide and nucleotide sequences regarding secreted Campylobacter jejuni proteins.

BACKGROUND OF INVENTION

1. Field of the Invention

The invention relates to Campylobacter jejuni gene products and immunogenic fragments of the gene products useful as component(s) of a pharmaceutical formulation capable of eliciting an anti-Campylobacter jejuni immune response. The invention also relates to a method of using inducing an anti-Campylobacter immune response by the administration of C. jejuni-secreted, flagellar gene co-regulated gene products or immunogenic fragments of the gene products.

2. Description of the Related Art

C. jejuni is a leading cause of diarrheal disease worldwide and a documented threat to US military personnel (Taylor, 1992; Tauxe, 1992). The symptoms of Campylobacter enteritis include diarrhea, abdominal pain, and fever and often accompanied by vomiting. Stools usually contain mucus, fecal leukocytes and blood, although watery diarrhea is also observed (Cover and Blaser, 1999). However, despite the importance of this organism to human disease, there are no licensed vaccines against C. jejuni.

Although Campylobacter infection is treatable with antibiotics, an effective vaccine formulation against the organism is a preferred method for disease prevention. Vaccine administration is especially desirable for travelers to regions of the world where Campylobacter is endemic. However, there are currently no licensed vaccines for this organism. Further hampering efforts in anti-Campylobacter vaccine development is the potential initiation of Guillain-Barre Syndrome (GBS) individuals exposed to Campylobacter (Kuroki, et al, 1991). However, because of the importance of flagellin in Campylobacter virulence, these genes have been promising in the development of anti-Campylobacter immunity (U.S. Pat. No. 6,987,176 to Guerry, et al).

Campylobacter posses a single polar flagella that has been shown to be critical for intestinal colonization and invasion (Wassennar, et al, 1991; Yao, et al, 1994). Flagellin has been shown to be the immunodominant antigen during human and animal infection and is required for colonization in vivo (Guerry, et al, 2000). Flagellar biosynthesis is regulated in a hierarchical fashion with genes expressed in the order in which they are required for the assembly of the flagellum. The production of flagella, however, requires significant expenditure of energy. Therefore, the regulation of these genes is of critical importance to the organism. However, unlike other bacterial species, only three sigma factors have been identified Campylobacter jejuni (σ⁷⁰, σ⁵⁴ and σ²⁸) (Parkhill, et al, 2000). These observations suggested that a number of Campylobacter genes are coordinately regulated.

Among members of the family Enterobacteriaceae, the genes flhC and flhD are the initial regulators of the flagellar regulatory cascade (Macnab, 2003). Within this scheme, a feedback mechanism ensures the correct order of flagellar gene expression. In Campylobacter jejuni, which lacks the flhC and flhD regulators, the genes in the flagella regulon expressed intermediate and late in the flagella regulatory cascade are controlled by the sigma factors σ⁵⁴ and σ²⁸, respectively.

Based on studies using the flhA gene and the gene fliA in the C. jejuni strain NCTC 11168, it has been observed that some genes of unknown functions, but not appearing to be directly involved in flagella function, were also co-regulated along with those genes associated with flagella function (Parkhill, et al, 2000); Carillo, et al, 2004). The flhA gene is expressed early in the cascade and which is involved in export of flagella proteins and the gene fliA encodes σ²⁸. Later studies have shown that many of these genes are also down-regulated in flagella mutants in C. jejuni 81-176, including the gene Cj0977 (Goon, et al, 2006).

The Cj0977 proteins, which are co-regulated with the flagella regulon, are 21.2 kDa and are 98% identical between the C. jejuni strains NCTC 11168 and 81-176 (Goon, et al, 2006). Furthermore, using a Cj0977 mutant, it was shown that Cj0977 resulted in significant attenuation of disease, using the ferret diarrhea disease model. However, the role of Cj0977 in virulence is still not understood. Furthermore, although Cj0977 is clearly important for virulence (Goon, et al, 2006), the protein has not been found to be secreted.

A putative σ²⁸-regulated gene, Cj0859c, encodes a protein with no homology to known proteins, and maps in a region of the chromosome that has been reported in a recent micrarray study to be variable among strains (Parker, et al, 2006). Reduced expression of this gene has been shown in a fliA mutant of NCTC 11168 (Carillo, et al, 2004). Analysis of this region in the C. jejuni genomes indicated that the putative σ²⁸ promoter was conserved, but that there was variation in the Cj0859c gene.

There is currently no effective anti-Campylobacter vaccine. Therefore, the identification of new anti-Campylobacter immunogenic formulations is of critical importance.

SUMMARY OF INVENTION

An aspect of this invention is a composition with homology to the Campylobacter jejuni protein Cj0859c that is normally co-regulated with C. jejuni flagellar proteins. The inventive composition can be isolated and prepared from natural C. jejuni isolates or be recombinantly produced. Included in the inventive composition are alternative forms of the same protein.

Another aspect of this invention is a method of inducing an immune response against Campylobacter by the administration of Cj0859c.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1. Phylogenetic tree based on protein sequences encoded by alleles of the fspA gene.

FIG. 2. Secretion of FspA.

FIG. 3. Illustration of requirement for minimum flagella structure for secretion of FspA.

FIG. 4. Interaction of FspA proteins with INT407 cells.

FIG. 5. Apoptosis induction by FspA2.

FIG. 6. Illustration of IgG and IgA response to FspA1

FIG. 7. Illustration of IgG and IgA response to FspA2.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

It has been observed that a number of Campylobacter jejuni genes of unknown function are nonetheless co-regulated with flagellar gene expression. These include the genes: Cj0859c (both A1 and A2 forms); Cj0243c; Cj1476; Cj1467; Cj1650; Cj1450; Cj1656c; Cj0391c. FlaC is secreted by not co-regulated with flagellar gene expression. Because of the importance of these genes in the pathogenesis of Campylobacter jejuni, flagella co-regulated genes that encode polypeptides that are secreted and are therefore accessible to the host immune response may be important immunologically. Therefore, an aspect of this invention is the use of these gene products in the development of anti-Campylobacter jejuni formulations.

Microarray analysis was conducted on these genes in order to ascertain the coordinate expression of these C. jejuni genes. The microarray assay contained PCR amplicons representing 1503 C. jejuni open reading frames. Most genes were sequenced using DNA from the C. jejuni strain NCTC 11168 (Parkhill, et al, 2000) or the strain 81-176. All predicted flagellin genes were included except flgI (Cj1462), flgA (Cj0769c) and flgM (Cj(1464). The result of this analysis is illustrated in Table 1.

In Table 1, bioinformatic analysis of the scanned arrays was performed using Microarray Suite version 5.1™ (Affymetrix). Duplicate microarray hybridizations were done on two independent preparations of RNA from each strain. The mean and standard deviations for the mutants in the flagella genes was calculated from the four microarray experiments. A change in signal was considered differentially regulated if the statistically significant change in expression was greater than 1.5-fold. The results are expressed as the fold difference in expression of the mutant compared to the wildtype in log₂. Thus, a sample reported as “−2” is a four-fold reduction in the mRNA levels in the mutant compared to wildtype; “−3” indicates an eight-fold reduction. The genes listed in Table 1 are not required for flagella biogenesis but were nonetheless 2 to greater than 250-fold down-regulated in strains with mutation in genes known to be involved in flagella biogenesis indicating their co-regulation with flagellar genes indicating their flagellar co-regulation. The characteristics of one of the genes listed in Table 1, Cj0977, was previously described (Goon, et al, 2006).

The data in Table 1 indicates that the genes Cj0859c; Cj0391; Cj1450; Cj1650; Cj 1656c; Cj0243c; Cj 1476; Cj 1728c; Cj0040 are co-regulated with flagellar genes. The data illustrated in Table 1 is consistent with the notion that Cj0859c is under the control of σ²⁸ since there is reduced gene expression (i.e., RNA) detected in fliA (σ²⁸) mutant because of feedback in the flagella regulon. Additionally, it has been previously shown that FlaC is secreted through the flagella filament (Song, et al, 2004) but it has not been previously shown to show any co-regulation with flagella.

TABLE 1 Promoter flgR flgS rpoN fliA flgA Cj0045c −3.8 −0.7 −2.9 −4.7 −1.1 C1025c −2.1 −2.4 −1.7 0.3 0.5 Cj1034c −1.8 −2.6 −1.7 −2.3 −0.8 Cj0040 σ⁵⁴ −7.5 −0.1 −8.7 1.8 0.5 Cj0243c σ⁵⁴ −4.2 −2.6 −5.8 1.4 −0.1 CjB0814 σ⁵⁴ −4.4 −3.5 −3.4 1.7 0.7 Cj1467 σ⁵⁴ −2.6 −1.6 −2.4 0.5 0.7 Cj1650 σ⁵⁴ −5.7 −4.5 −5.5 1 0.7 Cj1728c σ⁵⁴ −4.8 0.1 −3.9 2.2 1.4 Cj0977 σ²⁸ −2.7 −3.7 −2.1 −4.2 −0.4 Cj0859c σ²⁸ −2.7 −3.8 −2.9 −5.4 −1 Cj1450 σ²⁸ −1.2 −2.1 −0.5 −1.5 −0.8 Cj1656c σ²⁸ −0.6 −2.8 −1.1 −7.5 −0.4 Cj0391 σ²⁸ −0.2 −1.2 −1.2 −2 −0.7 Cj0720/flaC 0.2 −1.3 −0.1 0.2 −1.6

Also illustrated in Table 1, the genes Cj0040 and Cj0977 are not known to be secreted and therefore are not suitable as immunogenic candidates. Additionally, Cj 1728c is likely an inner membrane protein and is therefore also not likely to be able to be highly immunogenic. However, the proteins Cj0391; Cj 1450; Cj 1650; Cj0243c and Cj1476, like Cj0859c, are co-regulated with flagellar genes as well as likely to be secreted from the bacteria. Further analysis of Cj0859c revealed this moiety to be an important candidate against Campylobacter. The gene encoding Cj0859c has been termed “flagella secreted protein A” (fspA).

EXAMPLE 1 Characterization of Fsp

Characterization of the gene locus was conducted by DNA sequence analysis of PCR products derived from a collection of isolates. The variation of fspA by DNA sequence analysis of polymerase chain reaction (PCR) products generated from a collection of isolates from diverse geographical locations is illustrated in FIG. 1. In obtaining the data illustrated in FIG. 1, The Cj0859c-Cj0860 region of the chromosome of C. jejuni strains was PCR amplified using primers pg06.14 (SEQ ID. No. 5) and pg06.15 (SEQ ID. No. 6). Primer pg06.14 bound to the pabA gene (Cj0861) and pg06.15 bound to murA (Cj0858c). Amplicons were subjected to DNA sequence analysis using Big Dye Chemistry on an Applied Biosystems Model 3100 DNA™ sequencer and the sequences were assembled using Sequencher 4.5™ (Gene Codes). Each consensus sequence was manually inspected for quality assessment of the assembly. The Cj0859c gene sequence was identified and the biological sequences compared using commercially available software.

As shown in FIG. 1, two overall clusters of Cj0859c alleles are evident. The FspA1 cluster, which included 81-176, NCTC 11168 and RM1221, comprised 32% of the total strains (13/41). The FspA2 cluster comprised 68% of the total strains (28/41). The FspA2 cluster includes TGH9011, which was originally reported to lack Cj0859c based on micro array analysis using the NCTC 11168 allele as probe (36). The allele found in TGH9011, however, is truncated (i.e., is not detectable by immunoblot). The FspA1 proteins share a minimum of 81.7% identity within the group, and the FspA2 proteins share a minimum of 95.1% identity. There appeared to be no association of allele type and geographical isolation, although all of the Thai isolates examined contained the FspA2 allele.

EXAMPLE 2 Production of FspA Construct

Construction of GST-his-Fsp A₈₁₁₇₆ was conducted by was amplifying the fspA81176 gene from 81-176 by polymerase chain reaction (PCR). The template was DNA from strain 81-176 and the primers were: pg05.53 (SEQ ID. No. 7) and pg05.54 (SEQ ID. No. 8). These primers included sequences for cloning into pET41-EK LIC™, a vector that allows fusion to both a GST tag and hexahistidine tag (EMD Bioscience, Madison, Wis.). The 429 bp amplicon was purified using Qiaquick™ PCR purification columns (Qiagen, Valencia, Calif.) and ligated to pET41-EK LIC as directed by the manufacturer, and transformed into NovaBlue™ GigaSingles™ cells (EMD Biosciences). Several resulting clones were sequenced and one, which showed the predicted sequence, was selected for protein purification. The GST-his-Cj0859c protein (SEQ ID No. 18) was purified by nickel chromatography. The nucleic acid sequence encoding the GST-his-Cj0859c polypeptide is SEQ ID No. 17.

The FspA protein from 81-176 was also expressed as a histidine-tagged protein in E. coli for biological experiments as follows. The gene was PCR amplified from 81-176 using primers DR101 (5′-CCATATGCAAATTAACAATTCCTTAAATAGC-3′) and DR102 (5′-GGGATCCTCAAGCTTTGTTGGCTTTGGAGTTC-3′) and HF2 DNA polymerase (Clontech, Mountain View, Calif.). The resulting amplicon was digested with NdeI and BamHI and cloned into NdeI-BamHI-digested pET-19b (Novagen, San Diego, Calif.) in E. coli DH5α. The amino acid sequence of the histidine-tagged FspA1 (i.e., 81-176) is SEQ ID. No. 14, which is encoded by the nucleic acid sequence of SEQ ID No. 13.

FspA from CG8486 was expressed as a histidine-tagged protein in pET-19b using primers DR103 (5′-CCATATGAAAATAGATACTTTGACAAAAAATTTTAGC-3′) and DR102 (shown above), as described above for 81-176. The amino acid sequence of the histidine tagged FspA2 (i.e., CG8486) is SEQ ID. No. 16, which is encoded by the nucleic acid sequence of SEQ ID No. 15.

A mutant in fspA₈₁₁₇₆ was constructed using a Tn5 based in vitro transposition with a cat cassette as previously described (18). The in vitro reaction was performed according to manufacturer's instructions with a clone from a Sau3A1 partially digested ordered genomic library of 81-176 called pLCH8-63 as the target DNA. This clone contained the region of the 81-176 chromosome that corresponded to genes Cj0856c-Cj0860.

The reaction products were transformed into E. coli DH5α and plasmid DNAs from individual transformants were sequenced using primers that read out from within the cat cassette to determine the insertion point and the orientation of the transposon within the gene. A plasmid was selected in which the cat cassette had inserted 259 bp from the translational start of fspA in the same orientation as fspA. This plasmid was used to electroporate C. jejuni 81-176 with selection on Muller Hinton agar supplemented with chloramphenicol (15 μg/ml). The successful mutation of fspA was verified by PCR with primers bracketing the Cm^(r) insertion point to confirm that the DNA had undergone a double crossover. This mutant was called PG2572.

EXAMPLE 3 Secretion of Cj0859c

The ability of the Cj0859c (FspA) to be secreted was demonstrated. This study was conducted by western blot analysis using whole cells of C. jejuni 81-176 as a source of antigen as well as an isogenic insertional mutant of fspA₈₁₁₇₆. The blots were probed with rabbit polyclonal antiserum against a recombinant form of the protein (GST-his-FspA₈₁₁₇₆). See Example 2 for production of GST-his-FspA₈₁₁₇₆.

As illustrated in FIG. 2, the presence of a band in wildtype 81-176 with an apparent M_(r) of approximately 18 kDa, slightly larger than the predicted M_(r) of FspA₈₁₁₇₆. A histidine-tagged version of this protein expressed in E. coli also migrated aberrantly in SDS-PAGE (data not shown). This band was missing in the fspA₈₁₁₇₆ mutant and appeared to be over expressed when the mutation was complemented in trans. Since C. jejuni is known to secrete multiple proteins through flagella, we examined supernatants for the presence of Cj0859c.

FspA₈₁₁₇₆ was found in supernatants of 81-176 cultures and the complement of the mutant, but not in supernatants of the fspA mutant (FIG. 2A). Additional cross-reacting bands were also observed in some supernatant preparations and may represent processing events, degradation products, or cross-reacting proteins. To control for possible cell leakage, whole cell and supernatant preparations of 81-176 were immunoblotted with antibodies to recombinant forms of three other proteins, as shown in FIG. 2B. These were Cj0977, another σ²⁸-regulated cytoplasmic protein that is not secreted (Goon, et al, 2006), Omp18, a lipoprotein (Burnens, et al, 1995) and Omp50, an outer membrane protein (Bolla, et al, 2000). These proteins were readily detected in whole cells, but not in the supernatant preparations.

It was further determined that the FspA₈₄₈₆ protein is secreted from 81-176 when the gene is supplied in trans (see Example 2). In these studies, the fspA gene and its σ²⁸ promoter were PCR amplified from 81-176 using the following primers: pg05.133 (SEQ ID. No. 11) and pg05.134 (SEQ ID. No. 12. These primers added BamHI and EcoR1 sites, respectively. The resulting 744 bp amplicon was digested with BamHI and EcoRI (New England Biolabs, Beverly, Mass.) and cloned into similarly digested pRY107 (50). After confirmation that the clone was correct by DNA sequence analysis, the plasmid was transformed into DH5α cells carrying RK212.2. The resulting cells were used as donors to transfer conjugatively the complementing plasmid, pCE2575, into PG2166, the Cj0859c mutant, with selection on kanamycin and chloramphenicol.

It was observed that the FspA₈₄₈₆ protein can also found in the supernatant of cultures of CG8486, as shown in FIG. 2C, but did not show the aberrant migration observed with FspA₈₁₁₇₆. The fspA gene and its σ²⁸ promoter from CG8486 were inserted into the astA gene of 81-176 to generate PG2662. The two forms of FspA can be visualized in the supernatant of this strain by immunodetection with anti-FspA₈₄₈₆ antiserum (FIG. 2C). Only FspA₈₄₈₆ can be visualized in the supernatant of strain PG2663, the fspA₈₁₁₇₆ mutant of 81-176 containing fspA₈₄₈₆ inserted into astA. Cj0859c or fspA has been reported to be missing in several strains of C. jejuni by micro array analysis, including ATCC 43431 (TGH9011)(see Parker, et al, 2006; Poly, et al, 2005 and Poly et al, 2004). The gene was also absent in the sequenced strains of Campylobacter coli, Campylobacter upsaliensis, Campylobacter lari, and Helicobacter spp. Cj0859c was not detectable in whole cell immunoblots (data not shown) or supernatants of either C. jejuni TGH9011 or a C. coli strain, VC167 T2 (FIG. 2D). However, when pCE2575 carrying fspA₈₁₁₇₆ was transferred conjugatively into these strains, FspA₈₁₁₇₆ protein could readily be detected in both whole cells (data not shown) and in cell supernatants (FIG. 2D) indicating that the requisite machinery was present in these other Campylobacter strains to secrete the FspA₈₁₁₇₆ protein. Doublets of the FspA₈₁₁₇₆ protein were also observed in supernatants from these strains, as seen in FIG. 3D.

Song et al. (41) showed that FlaC secretion to the supernatants was not observed in C. jejuni TGH9011 mutants lacking hook (flgE) and basal body structures (flgF). We further examined secretion of FspA₈₁₁₇₆ from similar mutants, as shown in FIG. 3. The results indicate that neither FspA₈₁₁₇₆ nor FlaC was secreted in 81-176 mutants in flgE, flgI, encoding the P ring subunit, or flgK, encoding the hook-filament junction protein. Both proteins were secreted from a mutant in fliD lacking the filament cap protein. Therefore, secretion of FspA₈₁₁₇₆ requires a minimum flagella structure.

EXAMPLE 4 The Role of Cj0859c in Bacterial Virulence

Mutation of fspA₈₁₁₇₆ does not affect 81-176 adherence or invasion of INT407 cells. There was no significant difference between wildtype 81-176 and an fspA::cat mutant, which was fully motile, in terms of adherence (P=0.56) to or invasion of INT407 cells (P=0.61).

Recombinant his-tagged FspA₈₄₈₆ and FspA₈₁₋₁₇₆ proteins were added to a monolayer of INT407, incubated for 2 h, and washed extensively. The monolayer was lysed and the proteins separated in 12% SDS-PAGE gels and immunodetected. The results, shown in FIG. 4. In FIG. 4, Hexahistidine-tagged recombinant FspA1 or FspA2 (SEQ ID No. 14 and 16, respectively) were added to a monolayer of INT407 cells, which were then incubated for 4 hours at 37° C. After washing, an aliquot of a lysate was electrophoresed on a 12.5% SDS-PAGE gel, transferred to a nitrocellulose membrane and probed with anti-histidine-tagged mouse monoclonal antibody. In FIG. 4, Lane 1 shows recombinant FspA1; lane 2, INT407 cells plus 50 μg FspA1; lane 3, INT407 cells plus 5 μg FspA2; lane 4, INT407 cells plus 10 μFspA2; lane 5, INT407 cells plus 25 μg FpA2; lane 6, INT407 cells plus 50 μg FspA2; lane 7, recombinant FspA2; lane 8, recombinant FspA2. The results illustrated in FIG. 4, indicated that FspA₈₄₈₆ remained associated with the monolayer, while FspA₈₁₁₇₆ could not be detected in the lysate. These results illustrate that FspA₈₄₈₆, but not FspA₈₁₁₇₆, binds to INT407 cells.

Additionally, FspA₈₄₈₆ but not FspA₈₁₁₇₆ causes induction of apoptosis of INT407 cells. Recombinant his-tagged FspA₈₄₈₆ protein, but not recombinant his-tagged FspA₈₁₁₇₆ protein, caused induction of apoptosis in INT407 cells after 4 h incubation, as shown in FIG. 5. Moreover, there was a clear dose response to the recombinant FspA₈₄₈₆ protein. Addition of 5 μg of recombinant FspA₈₄₈₆ resulted in 11.9%±4.7% of the cells in early apoptotic stage (P=<0.05 compared to untreated INT407 controls). Addition of increasing amounts of FspA₈₄₈₆ from 10 μg to 50 μg resulted in a range of 15.4±2.4% to 30.9±4.8% of the cells in early apoptosis by 4 h (P<0.001). In contrast, addition of 50 μg of FspA₈₁₁₇₆ to the monolayer showed no differences compared to untreated controls. The kinetics of induction of apoptosis was markedly quicker than that caused by CDT (Cortes-Bratti, et al, 2001; Gelfanova, et al, 1999; and Hickey, et al, 2005). Membrane preparations (a total of 10 μg total protein) from 81-176 (CDT+) caused apoptosis in only 6.6±3.0% of the cells in 4 h and 17±8% by 24 h. Membranes from a cdtA mutant of 81-176 had no effect, as previously reported (Hickey, et al, 2000; Hickey, et al, 2005).

EXAMPLE 5 Immunogenicity of FspA1 and FspA2

A murine study were undertaken in order to evaluate the immunogenicity and potential protective efficacy of the inventive anti-FspA constructs. In the study, adult female BALB/c mice were lightly anesthetized with isoflurane and immunized intranasally with 30 μl of PBS containing the FspA1 or FspA2 protein alone or a mucosal adjuvant LTR192G. The experimental groups are illustrated in Tables 2 and 3.

TABLE 2 Experimental groups for FspA1 Group FSPA1 (μg) LTR192G (μg) N 1 0 − 10 2 5 − 9 3 5 + 10 4 25 − 10 5 25 + 10 6 100 − 10 7 100 + 9

TABLE 3 Experimental groups for FspA2 Group FSPA1 (μg) LTR192G (μg) N 1 0 − 8 2 5 − nd 3 5 + 8 4 25 − 8 5 25 + 8 6 100 − 8 7 100 + 8

Three doses of vaccine were delivered at 14-day intervals (study days 0, 14 and 28). Seven (7) days after the last vaccination (study day 35) fecal pellets were collected to determine secretory IgA. Antigen-specific serum IgG was determined in tail blood that was collected 21-22 days (study day 49-50) after last vaccination. ELISA determined antigen-specific responses. The IgG and IgA responses are illustrated in FIG. 6 for mice immunized with FspA1 and FIG. 7 for mice immunized with FspA2. The data presented in FIGS. 6 and 7 are presented as group geometric mean titer (natural log_(e)) and standard deviation.

All animals were challenged (study day 58) intranasally with 3×10⁹ du of C. jejuni 81-176 for mice immunized with FSPA1 or C. jejuni CG8486 for mice immunized with FSPA2. Following challenge, animals were followed for 6 consecutive days for the development of the infection-associated illness. Based on the severity of sickness a score was assigned to each animal as follows:

0=No apparent illness

1=ruffled fur

2=ruffled fur and hunched back

3=dead

A daily sickness index, and then group average indices were determined and vaccine efficacy was calculated as: (Control−vaccinated)/(Control)×100. Efficacy is represented in Table 4, for mice immunized with FspA1, and in Table 5, for mice immunized with FspA2.

As illustrated in FIG. 6A, FspA1 induced a robust vaccine dose dependent serum IgG response. This response was further enhanced by inclusion of a mucosal adjuvant LTR192G. Animals immunized with PBS showed only low levels of anti-FSPA1 IgG responses (mean+2 standard deviations=<1:500). Based on this cut off, all animals in all groups were categorized as IgG responders.

Similar to serum IgG, a robust mucosal IgA response was detected after vaccination (see FIG. 6B). Interestingly, LTR192G had a greater adjuvant effect on mucosal IgA response than observed for IgG. Animals immunized with PBS showed no detectable levels anti-FSPA1 fecal IgA responses (mean+2 standard deviations=<1:4). Based on this cut off, all animals in all groups were categorized as sIgA responders.

As illustrated in Table 4, FspA1 exhibited significant protective efficacy against C. jejuni challenge. As shown in Table 4, even without adjuvant, over 50% efficacy was observed, with co-administration of adjuvant enhancing the protective efficacy further.

TABLE 4 FspA1 efficacy in mice challenged with C. jejuni 81-176 Illness index Group FSPA1 (μg) LTR192G (μg) (mean ± sd) Efficacy ((%) 1 0 − 1.14 ± 0.22 n/a 2 5 − 0.94 ± 0.21 17 3 5 + 0.78 ± 0.20 31 4 25 − 0.59 ± 0.56 48 5 25 + 0.38 ± 0.17 67 6 100 − 0.47 ± 0.13 59 7 100 + 0.32 ± 0.16 71

As illustrated in FIG. 7, animals immunized with FspA2 exhibited a dose dependent serum IgG response (FIG. 7A), with administration of 25 μg of vaccine alone inducing a low level IgG response (50% responders). Conversely, 100 μg induced a potent IgG repose in all animals. Animals immunized with PBS alone showed only low levels of anti-FspA2 IgG responses (mean+2 standard deviations=<1:100). Administration of FspA2 with LTR192G a robust IgG response, even at the 5 μg dose.

Referring to FIG. 7B, only 100 μg dose was able to induce mucosal IgA when delivered alone. As observed for IgG responses, co-delivery of vaccine with LTR192 resulted in equivalent levels of antigen-specific sIgA, even down to the 5 μg dose. Animals immunized with PBS showed no detectable levels anti-FSPA2 fecal IgA responses (mean+2 standard deviations=<1:4). The adjuvant effect, in these studies, was more pronounced in the mucosal IgA response than in the serum IgG response.

Animals immunized with 5 μg of FspA2 showed only minimal protection, as illustrated in Table 5. However, moderate protection was evident at higher doses with the adjuvant LTR192G providing some enhancement of protection.

TABLE 5 FspA2 efficacy in mice challenged with C. jejuni 8486 Illness index Group FSPA1 (μg) LTR192G (μg) (mean ± sd) Efficacy ((%) 1 0 − 1.23 ± 0.25 n/a 2 5 − nd 3 5 + 1.06 ± 0.34 13.8 4 25 − 1.05 ± 0.27 14.6 5 25 + 0.79 ± 0.31 35.8 6 100 − 0.77 ± 0.20 37.4 7 100 + 0.64 ± 0.21 47.9

These studies illustrate the utility of these constructs as components, alone or in combination with other moieties, of vaccines against Campylobacter. Accordingly, the inventive constructs can be used in methods for the induction of protective anti-Campylobacter immunity.

A prophetic method for the induction of the anti-C. jejuni mediated response in humans contains the following steps:

-   -   a. administration of immunogen comprising FspA1 or FspA2, or         immunogenic fragments, thereof, with or without a tag, such as         histidine or GST. If a boosting dose or doses are to be given         this first administration of immunogen is a priming dose. The         immunogen can be derived from isolated native polypeptide or         recombinantly produced FspA, or FspA fragments. The immunogen         can be administered orally, nasally, subcutaneously,         intradermally, transdermally, transcutaneously intramuscularly,         or rectally. The range of a unit dose of immunogen is 50 μg to 1         mg of immunogen. The immunogen is administered in any number of         aqueous buffered solutions with or without carrier protein or         adjuvant. The adjuvant can be any number of potential adjuvants,         including LTR 192G.     -   b. The inventive method also contemplates immunization with or         without administration of subsequent boosting. The boosting step         comprises the administration of, subsequent to a priming dose, 1         to 4 boosting doses with a unit dose range of 50 μg to 1 mg of         immunogen in a buffered aqueous solutions.

Alternative embodiments of the inventive method include inserting nucleotide constructs encoding FspA1 or FspA2, or fragments thereof, into an expression system capable of expression in mammalian subjects. In this embodiment, the expression system can be a viral or DNA expression vector. Another alternative embodiment of the inventive method is to induce immunity by administering a live attenuated carrier strain of bacteria transformed with a suitable viral or DNA expression system that contains one or more nucleic acid sequences encoding one or more of the polypeptides FspA1, FspA2, or fragments thereof. The expression system contemplated is capable of expressing in the selected bacteria carrier.

REFERENCES

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Having described the invention, one of skill in the art will appreciate in the appended claims that many modifications and variations of the present invention are possible in light of the above teachings. It is therefore, to be understood that, within the scope of the appended claims, the invention may be practiced otherwise than as specifically described. 

What is claimed is:
 1. An immunogenic composition comprising an isolated Campylobacter jejuni flagella secreted protein A, comprising amino acid sequence set forth in SEQ ID NO.
 4. 2. The immunogenic composition of claim 1, wherein said flagella secreted protein A is a recombinant polypeptide.
 3. The immunogenic composition of claim 2, wherein said polypeptide contains a histidine tag.
 4. The immunogenic composition of claim 2, wherein said polypeptide is encoded by the nucleic acid sequence set forth in SEQ ID No.
 3. 5. The immunogenic composition of claim 3, wherein said polypeptide is set forth in SEQ ID No.
 16. 6. The immunogenic composition of claim 5, wherein said polypeptide is encoded by the nucleic acid sequence set forth in SEQ ID No.
 15. 7. A method of inducing an immune response against Campylobacter jejuni comprising the steps of administering a dose of said immunogenic composition of claim
 1. 8. The method of claim 7, comprising the addition step of administering one or more boosting doses subsequent to said priming dose wherein said boosting dose is comprised of the same said immunogenic composition as administered in said priming dose.
 9. The method of claim 7, wherein said composition is a recombinant polypeptide with the amino acid sequence set forth in SEQ ID No.
 4. 10. The method of claim 7, wherein said dose is administered by a method selected from the group consisting of intranasally, subcutaneously, transdermally, orally and intravenously.
 11. The method of claim 8, wherein said boosting dose is administered by a method selected from the group consisting of intranasally, subcutaneously, transdermally, orally and intravenously.
 12. The method of claim 9, wherein said recombinant polypeptide contains a histidine tag.
 13. The method of claim 9 wherein said amino acid sequence is encoded by a nucleic acid sequence set forth in SEQ ID No.
 3. 14. The method of claim 12, wherein said polypeptide is set forth in SEQ ID No.
 16. 15. The method of claim 13, wherein said nucleotide sequences encoding said polypeptide sequences is inserted in an expression vector wherein said expression vector is selected from the group consisting of plasmid and viral expression vectors and wherein said expression vector is functional in mammalian subjects and wherein said polypeptide sequence is expressed.
 16. The method of claim 13, wherein said nucleotide sequences are inserted in a plasmid or viral expression vector system and expressed in a live, attenuated strain of carrier bacteria.
 17. The method of claim 16, wherein said attenuated strain of carrier strain is selected from the group consisting of Escherichia coli, member of the genus Shigella, member of the genus Campylobacter, member of the genus Salmonella, member of the genus Vibrio. 